|  Help  |  About  |  Contact Us

Allele : Mfsd2a<em1Chgu> MFSD2 lysolipid transporter A, lysophospholipid; endonuclease-mediated mutation 1, Chenghua Gu

Primary Identifier  MGI:6120542 Allele Type  Endonuclease-mediated
Gene  Mfsd2a Strain of Origin  (C57BL/6J x SJL/J)F1/J
Is Recombinase  false Is Wild Type  false
molecularNote  An A to C mutation resulting in a D96A substitution was inserted in exon 3 by CRISPR/Cas9 mediated recombination. Immunohistochemical and western blot analysis indicated no change in protein expression in the brains of homozygous mice compared to wild-type controls. Altered lipid profiles in the brains of homozygotes indicate this mutation abolishes the lipid transport function of the gene.
  • mutations:
  • Single point mutation
  • synonyms:
  • Mfsd2a<D96A>,
  • Mfsd2a<D96A>
Quick Links:
 
Quick Links:
 

1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

2 Publication categories

Trail: Allele